Class Class II

Quadsense (Quadsense and Quadsense Pro) (K252524)

K252524 2025-09-09 Special
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Description

Quadsense (Quadsense and Quadsense Pro) by Eventum Orthopaedics, Ltd., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252524
Clearance Date2025-09-09
Clearance TypeSpecial
Product CodeONN
Regulation Number882.4560

Categories

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